Chunk #16 — Discussion

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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

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While most CNVs occurred only in single patients in our study, there was some overlap with the findings from the earlier CNV studies in ADHD (15–18), and some CNVs have been linked to ADHD in other ways (see Table S6 in the online data supplement). These CNVs mark genes that might be of particular relevance to ADHD and would make good candidates for further study.