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Recent studies suggest that copy number variation in the human genome is extensive and may play an important role in susceptibility to disease, including neuropsychiatric disorders such as schizophrenia and autism. The possible involvement of copy number variants (CNVs) in bipolar disorder has received little attention to date.

archives of general psychiatry

Rare Copy Number Variants&lt;subtitle&gt;A Point of Rarity in Genetic Risk for Bipolar Disorder and Schizophrenia&lt;/subtitle&gt;&lt;alt-title&gt;Rare Copy Number Variants&lt;/alt-title&gt;