Gene copy number variation (CNV) refers to the presence of multiple copies of a gene family within a genome resulting from duplications, deletions, or rearrangements. In general, CNV may result from ...
Copy number variation (CNV) is a type of structural variation ranging from 50 to several million base pairs (bp) 1,2,3,4,5. It is an unbalanced variation where a segment of the human genome can be ...
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