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Chunk #41 — Glossary

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Polygenic risk scores in psychiatry: Will they be useful for clinicians?
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yes

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Copy number variant (CNV): Copy number variation is a phenomenon in which sections of the genome are deleted, repeated, or inverted and the number of repeats in the genome varies between individuals in the population. CNVs can contain whole genes or crucial regulatory elements which influence gene expression or may have no appreciable functional effect.