Seven overlapping CNVs shared in >4 individuals with CoA were identified. The chromosome 21 CNV locus was present in all familial CoA cases. It contains TRPM2, which was also identified in the sporadi
Filtered variant call format (VCF) data of Jinbuol (JBO, female), Samgwang (SG, male), two RIL individuals (JSRIL1 and JSRIL2), Nipponbare1, IndicaHR12, Kitaake, and Kasalath using resequencing data p
