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DNA Labs India

Microarray 60K (POC)+ Single Karyotying Test

DNA Labs India | ISO 9001:2015 Certified

Microarray 60K (POC)+ Single Karyotying Test

Short Name: Microarray 60K POC + Single Karyotying

Also known as: Chromosomal Microarray Analysis, CMA with Karyotyping

Microarray 60K (POC)+ Single Karyotying Test test available at DNA Labs India for ₹15,000. Uses Microarray Analysis, Cell Culture on Products of Conception, Peripheral blood of parents samples. Results in 7-9 days. Free home collection in 300+ cities across India.

DiagnosticAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect chromosomal abnormalities, gene duplications, and deletions that may be causing genetic conditions such as autism, intellectual disability, and developmental delays, aiding in accurate diagnosis and personalized care.

Test Code
3097
Price
₹15,000
Sample Type
Products of Conception, Peripheral blood of parents
Result Time
7-9 days
Fasting Required
No
Method
Microarray Analysis, Cell Culture
Step 1

Sample Collection

Ensure a doctor's prescription is available. No fasting required. Inform the lab about any medications or health conditions.

Method: Blood draw or tissue sample collection

Step 2

Laboratory Analysis

A small sample of blood or tissue will be collected by a trained professional using sterile techniques. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bleeding. Resume normal activities. Store samples as instructed for stability.

Timeline: 7-9 days

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. No special preparation or fasting is needed. Discuss any concerns with your healthcare provider.
2
During the Test:Sample collection takes a few minutes. For blood, a needle is used; for tissue, a small biopsy may be taken. The procedure is generally painless.
3
After the Test:Results are available in 7-9 days. Review results with your doctor or genetic counselor for appropriate next steps.

About This Test

Who Should Get This Test

The purpose of this test is to detect chromosomal abnormalities, gene duplications, and deletions that may be causing genetic conditions such as autism, intellectual disability, and developmental delays, aiding in accurate diagnosis and personalized care.

How to Prepare

  • Bring a valid doctor's prescription
  • Wear comfortable clothing for easy access
  • Inform about any allergies or bleeding disorders
  • Follow lab instructions for sample transport

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"As a gynecologist, I recommend this test for couples with recurrent miscarriages or abnormal prenatal findings to identify genetic causes and guide management."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeProducts of Conception, Peripheral blood of parents
ContainerSterile Container or Sterile Normal Saline Container
Collection MethodBlood draw or tissue sample collection

Sample Stability

Blood samples stable for 48 hours at room temperature
Tissue samples should be transported in sterile saline on cool packs
Avoid extreme temperatures during transport
Sample Rejection Criteria:
  • Insufficient sample volume
  • Contaminated or hemolyzed samples
  • Incorrect sample type or container
  • Missing prescription where required

Understanding Your Results

Results are interpreted by clinical geneticists to identify chromosomal abnormalities. A normal result indicates no detectable abnormalities, while abnormal results may indicate genetic conditions requiring further evaluation.
📊

Normal

No chromosomal abnormalities detected; genetic health is typical based on the test scope.

📊

Abnormal

Presence of chromosomal abnormalities such as deletions or duplications; genetic counseling and further testing recommended.

📊

Variant of Uncertain Significance (VUS)

Genetic change detected but clinical significance unclear; monitoring and family studies may be advised.

⚠️ When to Consult a Doctor:

If you or your child exhibits symptoms like developmental delay, intellectual disability, recurrent miscarriages, or birth defects, consult a healthcare provider for genetic testing and counseling.

Limitations

  • May not detect all genetic variants or single-gene disorders
  • Results require clinical correlation and genetic counseling
  • Turnaround time of 7-9 days may delay diagnosis

Risks & Considerations

  • Minor bruising or soreness at the collection site
  • Rare risk of infection
  • Emotional impact of results; genetic counseling recommended

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Incorrect sample type
  • Hemolyzed blood samples

Frequently Asked Questions

What is Microarray 60K (POC)+ Single Karyotying?
It is a genetic test that combines microarray analysis and karyotyping to detect chromosomal abnormalities, such as deletions and duplications, often used for conditions like autism or recurrent miscarriages.
How much does the test cost?
The cost is INR 15000 at DNA Labs India, with free home sample collection available across India.
What symptoms indicate the need for this test?
Symptoms include developmental delay, intellectual disability, autism spectrum disorder, recurrent miscarriages, birth defects, delayed growth, unexplained seizures, and abnormal facial features.
How is the test performed?
A small sample of blood or tissue is collected and analyzed in a lab using microarray and cell culture methods. Results are typically ready in 7-9 days.
Is a doctor's prescription required?
Yes, a doctor's prescription is generally required, except for surgery, pregnancy cases, or people planning to travel abroad.
What is the turnaround time for results?
Results are usually available within 7-9 days after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in many cities across India.
What are the risks of the test?
Risks are minimal and may include minor bruising at the collection site or rare infection. Emotional impact is possible, so genetic counseling is advised.
How accurate is the test?
The test is highly accurate for detecting chromosomal abnormalities, but it may not identify all genetic variants. Results should be interpreted by a geneticist.
What should I do if results are abnormal?
Consult a healthcare provider or genetic counselor for further evaluation, management options, and family planning advice.
Is the test covered by insurance?
Coverage varies by insurance plan. It is not typically covered under government schemes like PMJAY; check with your insurer for details.
Can this test be done during pregnancy?
Yes, it can be performed on products of conception or parental blood, but consult your doctor for appropriate timing and guidance.
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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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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