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DNA Labs India

Cord Blood For Karyotyping Test

DNA Labs India | ISO 9001:2015 Certified

Cord Blood For Karyotyping Test

Short Name: Cord Blood Karyotyping

Also known as: Cord Blood Chromosome Analysis, Neonatal Karyotyping, Umbilical Cord Blood Karyotype

Cord Blood For Karyotyping Test test available at DNA Labs India for ₹6,000. Uses Cell Culture on Cord Blood samples. Results in 7-9 days. Free home collection in 300+ cities across India.

Genetic TestNewborn🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect chromosomal abnormalities in newborns for early diagnosis and management of genetic disorders.

Test Code
2977
Price
₹6,000
Sample Type
Cord Blood
Result Time
7-9 days
Fasting Required
No
Method
Cell Culture
Step 1

Sample Collection

Ensure a doctor's prescription is available. No specific preparation required for the newborn.

Method: Cord Blood Collection

Step 2

Laboratory Analysis

Cord blood is collected from the umbilical cord after birth by a trained healthcare professional.

Step 3

Report Delivery

Apply pressure to the collection site if needed. Store sample as instructed for transport.

Timeline: 7-9 days

Patient Instructions

1
Before the Test:Obtain doctor's prescription. No fasting required.
2
During the Test:Sample collection from umbilical cord after birth.
3
After the Test:Monitor newborn as usual. Await results.

About This Test

Who Should Get This Test

To detect chromosomal abnormalities in newborns for early diagnosis and management of genetic disorders.

How to Prepare

  • Use sterile equipment
  • Collect in Sodium Heparin Vacutainer
  • Label sample correctly
  • Transport at ambient temperature

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Cord blood karyotyping is essential for early detection of genetic disorders in newborns, enabling timely intervention and genetic counseling for better outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeCord Blood
Sample Volume2 ml
ContainerSodium Heparin Vacutainer
Collection MethodCord Blood Collection

Sample Stability

Stable for 24 hours at room temperature
Avoid extreme temperatures
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Incorrect container
  • Contaminated sample

Understanding Your Results

Results indicate the chromosomal makeup of the newborn. Abnormalities may require further genetic counseling and medical evaluation.
📊

Normal Karyotype

No chromosomal abnormalities detected

📊

Abnormal Karyotype

Chromosomal abnormalities present, consult a geneticist

📊

Mosaicism

Mixed cell populations, may need further testing

⚠️ When to Consult a Doctor:

If results show abnormalities or if there are concerns about the newborn's development, consult a geneticist or pediatrician immediately.

Limitations

  • Cannot detect single gene disorders
  • Limited to chromosomal abnormalities
  • May not identify all structural variants

Risks & Considerations

  • Minimal risk from blood collection
  • Possible bruising at site
  • Rare infection risk

Interfering Factors

  • Contaminated sample
  • Improper storage or transport
  • Hemolyzed blood sample

Compare With Similar Tests

TestCord Blood For KaryotypingAmniocentesis KaryotypingFISH TestChromosomal MicroarrayNewborn Screening Panel
ComparisonCord Blood For KaryotypingPerformed during pregnancy, not on cord bloodFaster but targets specific chromosomesDetects smaller deletions/duplicationsTests for metabolic disorders, not chromosomes

Frequently Asked Questions

What is cord blood karyotyping?
It is a test that examines chromosomes in a newborn's cord blood to detect abnormalities.
Why is cord blood karyotyping performed?
To diagnose chromosomal disorders in newborns with symptoms like developmental delays or physical anomalies.
How is the sample collected?
Cord blood is collected from the umbilical cord after birth using a sterile vacutainer.
Is there any risk associated with the test?
Risks are minimal, such as slight bruising at the collection site.
How long does it take to get results?
Results are typically available within 7-9 days.
What do abnormal results mean?
Abnormal results indicate chromosomal abnormalities; consult a geneticist for interpretation and next steps.
Can this test detect all genetic disorders?
No, it only detects chromosomal abnormalities, not single gene disorders.
Is fasting required for the test?
No, fasting is not required.
How much does the test cost?
The cost is INR 6000 at DNA Labs India, with free home collection.
Is home collection available?
Yes, free home sample collection is available across many cities in India.
What should I do if results are abnormal?
Consult a healthcare professional or geneticist for further evaluation and counseling.
How accurate is cord blood karyotyping?
It is highly accurate for detecting chromosomal abnormalities when performed by experienced technicians.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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