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Chromosomal Array CNV+SNP, POC in Khar
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Overview
Chromosomal microarray analysis, also known as CNV+SNP (Copy Number Variation + Single Nucleotide Polymorphism), is a genetic test used on products of conception (POC), which is tissue from a miscarriage or termination of pregnancy. This advanced technique examines the chromosomes of the fetus for imbalances or abnormalities. Chromosomal microarray can detect small deletions or duplications of genetic material (CNVs) that traditional chromosome analysis might miss. Additionally, it can identify specific gene variations (SNPs) that might contribute to pregnancy loss. This information can be helpful for couples experiencing recurrent miscarriages to understand the potential cause and guide future family planning decisions.
Chromosomal Array CNV+SNP, POC Price in Khar
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Chromosomal Array CNV+SNP, POC with a clear pricing structure
The price of Chromosomal Array CNV+SNP, POC in Khar is ₹ 17,640
We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.
Frequently Asked Questions
This test allows laboratory to identify chromosomal aberrations which can lead to genetic disorders causing development disabilities and congenital anomalies.
This test is offered to patients suffering from conditions like unexplained seizures, developmental delay, dysmorphic features, psychiatric illness, neuromuscular conditions an autism spectrum disorders and multiple congenital abnormalities .
Chromosomal microarray analysis is a method to detect cytogenetic abnormalities. It measures gains and losses of DNA. Technique has higher resolution than karyotyping, does not require culture and has success rate of 98%. The technique uses over 60000 oligonucleotide probes and can detect deletions above 200 kb and duplications above 500 kb. However this technique will not detect low level mosaicism, balanced translocations, inversions or point mutations that may be responsible for the clinical phenotype. This test is offered to patients suffering from unexplained seizure disorder, growth delay, psychiatric illness, neuromuscular conditions an autism spectrum disorders.
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Why Metropolis?
Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.
We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.
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