Karyotyping by G-Banding-blood near me in Noida

Also referred as

Chromosome analysis

Karyotyping for Non-Hematological Malignancies

Constitutional Karyotyping

For men & women

Earliest reports in

312 hours

Contains

1 test

Test price:

₹3040

~~₹3200~~

5% off

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Know more about this test

The Karyotyping by G-Banding-blood is an advanced cytogenetic test used to examine the number, size, shape, and structure of chromosomes to detect genetic abnormalities. It uses a specialized G-banding staining technique, which produces characteristic light and dark banding patterns that help specialists identify missing, extra, or rearranged chromosomes. This test plays an important role in diagnosing inherited genetic disorders, chromosomal abnormalities, congenital anomalies (birth defects), infertility-related genetic conditions, recurrent pregnancy loss, and chromosomal abnormalities associated with certain non-hematological malignancies. This test is widely available with Tata 1mg labs at an affordable price in Noida.

Note: This test is not meant for the diagnosis of hematological malignancies (or Leukemia).

Samples required

Blood

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Why is this test booked?

Preparation for this test

Sample Collection

Who will collect your samples?

What does Karyotyping by G-Banding-blood measure?

The Karyotyping by G-Banding-blood examines the complete set of chromosomes in a blood sample to evaluate their number, size, shape, and structure. It detects numerical chromosomal abnormalities, such as extra or missing chromosomes (aneuploidy), as well as structural abnormalities, including deletions, duplications, inversions, translocations, and other chromosomal rearrangements.

This test helps identify constitutional (inherited or congenital) chromosomal abnormalities associated with genetic disorders, developmental delay, intellectual disability, congenital anomalies, infertility, recurrent pregnancy loss, and certain reproductive disorders. The results also provide valuable information for genetic counseling, reproductive planning, and determining whether additional genetic tests, such as FISH, chromosomal microarray, or genetic sequencing, may be required.

Test Information is reviewed by: Dr. Swati Gupta (Anand), MD Lab Medicine, MBBS and written by Shweta Prakash, MSc, BSc . The test details are for information purpose only. Consult a doctor before taking any test. Last updated on: 16th Jul 2026

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Karyotyping by G-Banding-blood test price for other cities

Price in	Bangalore	Rs. 3469
Price in	New Delhi	Rs. 2879
Price in	Hyderabad	Rs. 3039
Price in	Gurgaon	Rs. 2879
Price in	Mumbai	Rs. 3869

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FAQs related to Karyotyping by G-Banding-blood in Noida

What is the importance of getting the Karyotyping by G-Banding-blood test done?

This test can detect chromosomal abnormalities associated with congenital anomalies, developmental disorders, infertility, recurrent pregnancy loss, and inherited genetic conditions. It also helps guide genetic counseling and reproductive planning.

How is the test performed?

A trained phlebotomist collects a blood sample from a vein in your arm. In the laboratory, white blood cells are cultured to allow cell division. The chromosomes are then stained using the G-banding technique and examined under a microscope by specialists to evaluate their number and structure.

Is fasting required for the Karyotyping by G-Banding-blood test?

No, fasting is not required for this test. However, it is advised to follow your doctor's instructions thoroughly before getting this test done.

When should I get the Karyotyping by G-Banding-blood test?

The Karyotyping by G-Banding-blood is recommended if you have unexplained developmental delay, intellectual disability, congenital anomalies, infertility, recurrent pregnancy loss, poor obstetric history, or a family history of chromosomal disorders. Your doctor may also recommend this test when a chromosomal abnormality is suspected based on clinical findings or to evaluate reproductive risk.

How often should I get tested?

The frequency of this test depends on your individual circumstances. Your doctor will recommend the appropriate testing schedule based on your health, medical history, and any potential symptoms.

Can I schedule the Karyotyping by G-Banding-blood test online in Noida near me?

Yes. In Noida, you can schedule the Karyotyping by G-Banding-blood test near you with Tata 1mg Labs. The test is easy to book, cost-effective, and available with a comprehensive report.

Is a home sample collection facility available for the Karyotyping by G-Banding-blood test in Noida with Tata 1mg Labs?

Yes, home sample collection for the Karyotyping by G-Banding-blood test is readily available in Noida. Tata 1mg Labs allows you to choose a date and time that suits your schedule for sample collection.

How can I schedule the Karyotyping by G-Banding-blood test with Tata 1mg Labs in Noida?

If you want to schedule the Karyotyping by G-Banding-blood test with Tata 1mg Labs in Noida, the procedure is fairly easy and hassle-free. Follow these steps to book a test: 1). Visit the Lab Tests section on the Tata 1mg website. 2). Add the test you want to the cart. 3). Pick a time and date slot according to your convenience; however, do consider the necessary prerequisites while scheduling a test. 4). You will receive a notification with all the details once the test is scheduled.

What is the price of the Karyotyping by G-Banding-blood test at Tata 1mg Labs in Noida?

Tata 1mg Labs is a pocket-friendly platform for booking lab tests in Noida. The Karyotyping by G-Banding-blood test is available at an affordable price of Rs. 3040.

How long does Tata 1mg Labs take to give the reports of the Karyotyping by G-Banding-blood test in Noida?

We at Tata 1mg Labs recognize the value of prompt results. We strive to deliver test results with quick turnaround times so you can receive the information promptly. The reports of the Karyotyping by G-Banding-blood test in Noida are often provided in 312 hours.

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Contains 1 test

Karyotyping by G-Banding-blood

Report delivery

Standard time

312 hrs

For slots after 11 AM, report will be delivered in 336 hours.

Samples required

Blood

1 vial required

Our phlebotomist will draw a blood sample, typically from a vein in your inner elbow.

Preparations

A duly completed Chromosome Analysis, Karyotyping/ FISH Analysis Requisition Form (TRF - PAC/FR/04) is mandatory before sample collection.

Physician/doctor prescription, clinical indications, and clinical history are mandatory. Clinical details should be provided in the form of ultrasound findings, phenotypic features, family history, etc.

Please note: The reporting for the test may be delayed in case the TRF and Doctor prescription is not provided to the lab.

Why is this test booked?

To detect numerical chromosomal abnormalities, including the presence of extra or missing chromosomes.

To Identify structural chromosomal abnormalities such as deletions, duplications, translocations, inversions, and other rearrangements.

To diagnose constitutional chromosomal abnormalities in individuals with suspected genetic disorders, developmental delay, intellectual disability, or congenital anomalies.

To evaluate individuals with a family history of chromosomal disorders or help identify specific chromosomal abnormalities present in family members.

To assist in the investigation of infertility (in both males and females), recurrent pregnancy loss, recurrent miscarriages, stillbirth, poor obstetric history, delayed or abnormal puberty, and suspected balanced chromosomal rearrangements.

To aid in confirming chromosomal abnormalities in newborns with congenital anomalies or suspected genetic syndromes.

To detect acquired chromosomal abnormalities associated with selected non-hematological malignancies. This test is not meant for leukemia and other blood malignancies.

To support genetic counseling by providing chromosomal information that helps assess recurrence risk, reproductive planning, and the need for further genetic testing.

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