Recents studies in mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report the first gl
Additional file 3: Table S2. Variants identified in the 200 whole-genome sequences. This file provides details on all predicted and merged variants before applying validation approaches (in silico and
This is the genome-wide copy numbers (CNs) for every 1kb window in the genomes of nine Macaca species, including the Chinese rhesus (M. mulatta lasiota, CR), cynomolgus (M. fascicularis, CE), Tibetan
Copy number variations (CNVs) account for a significant proportion of inter-individual genomic variation. However, a majority of genomic variation studies have focused on single nucleotide variations
