Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve

Whole genome genotyping data in dbGAP format and copy number variant calls in dbVar format.

dbVar data includes CNV calls from cases with early onset bicuspid aortic valve disease (EBAV), cases from the International BAV Consortium (BAVCon), and controls from the dbGAP Wisconsin Longitudinal Study on Aging dataset (WLS).

dbGAP files are divided into 12 batches of genotypes from EBAV subjects (EBAV1-12):

1) PLINK output files (.map and .ped)

2) GenomeStudio Final Report files

3) One master pedigree file

4) dbGAP subject mapping files