Additional file 2: of Screening populations for copy number variation using genotyping-by-sequencing: a proof of concept using soybean fast neutron mutants

Copy number variants found in the 19 individuals subjected to aCGH. ID: the identifier of the mutant; CNV_type: the type of CNV (homdel = homozygous deletion, hetdel = hemizygous deletion, dup = duplication); chr: the chromosome on which the CNV is located; start: the starting position of the CNV; end: the end position of the CNV; kbp: the estimated size of the CNV in kbp; n_probes: the number of aCGH probes supporting this CNV; mean_log2: the mean log2 ratio of the probes across this CNV; found_by_GBS: whether or not this CNV was detected by the GBS approach. (CSV 6 kb)