copy number variations (cnvs)

How are CNVs Detected?

CNVs can be detected using various techniques such as array comparative genomic hybridization (aCGH), quantitative PCR, and next-generation sequencing (NGS). Each method has its advantages and limitations. For instance, aCGH is useful for detecting larger CNVs, while NGS can detect both small and large variations with high resolution.

Frequently asked queries:

What are Copy Number Variations (CNVs)?
How are CNVs Detected?
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