CNV identified by depth but can not be identified by snp allele frequency

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9.7 years ago

wangjiaqian ▴ 40

CNV identified by depth but can not be identified by snp allele frequency. Depth support that there is one allele of Amplification in chromosome arm. But SNP BAF of that region has no sign as an CNV(enriched at 0.5). My data is sequenced by Illumina(150X, exome, Agilent 50M). Is there any bias of capture system, or this phenomenon is normal?

Thank you for help!

genome CNV sequencing ASCAT • 1.7k views

ADD COMMENT • link updated 2.3 years ago by Ram 43k • written 9.7 years ago by wangjiaqian ▴ 40

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More details and some example data would be helpful. Exome data is notoriously noisy as a source of CNV estimates. Can you describe in more detail why you believe that there is a single copy amplification of that arm? Did you use a CNV caller? Which one. Also what are the variant allele frequencies there?

ADD REPLY • link updated 2.3 years ago by Ram 43k • written 9.6 years ago by Malachi Griffith 19k

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