Conrad.hg19.common.CNVs: Conrad et al common CNVs
In ExomeDepth: Calls Copy Number Variants from Targeted Sequence Data
Conrad.hg19.common.CNVs R Documentation
Conrad et al common CNVs
Description
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.
Format
A data frame with common CNV calls.
Source
Conrad et al, Origins and functional impact of copy number variation in the human genome, Nature 2010
ExomeDepth documentation built on Nov. 3, 2022, 5:05 p.m.
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| Conrad.hg19.common.CNVs | R Documentation |
Conrad et al common CNVs
Description
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.
Format
A data frame with common CNV calls.
Source
Conrad et al, Origins and functional impact of copy number variation in the human genome, Nature 2010
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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