Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature.

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This review article summarizes 10 years of published research on the range of neurodevelopmental and neuropsychiatric conditions seen in people who carry a 16p11.2 (BP4-BP5) deletion or duplication, helping families understand the variety of challenges that may be associated with their child's diagnosis.