Conrad.hg19.common.CNVs

<p>Positions of common CNV calls (detected in a panel of 42 sample) from the
Conrad et al paper (Nature 2010). This is build hg19 of the human genome.</p>

datasets

Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.

Vincent Plagnol

ExomeDepth

Calls Copy Number Variants from Targeted Sequence Data

Conrad.hg19.common.CNVs function

<p>A data frame with common CNV calls.</p>

Conrad.hg19.common.CNVs: Conrad et al common CNVs

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