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{"target":"http://pubannotation.org/docs/sourcedb/PMC/sourceid/5118444","sourcedb":"PMC","sourceid":"5118444","source_url":"https://www.ncbi.nlm.nih.gov/pmc/5118444","text":"CNVs were then used to construct a set of copy number variable regions (CNVRs). A CNVR was constructed by merging CNVs across samples that exhibited at least 50% pairwise reciprocal overlap in their genomic coordinates. For example, suppose we have two CNVs, CNV1 beginning at position a and ending at position b and CNV2 running from c to d with a \u003c c \u003c b \u003c d. If the reciprocal overlap between the two CNVs is at least 50% then they are merged into a CNVR which runs from a to d on the genome.","tracks":[]}