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Paper Details

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Am J Hum Genet
425
2012
CNV, CNVs, captured exons, copy-number variation, exome, exon, exons, gene, gene-coding regions, human, schizophrenia
Author NameAffiliation
Menachem FromerMount Sinai School of Medicine
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Datasets

Release 1.2