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
E. coli isolates 019S, 026F2, 026F3, and 128S were used as reference strains to call SNPs in each ST. Numbers in the distance matrix denote the numbers of SNPs between each sample pair. (XLSX)