In 2016, Green et al. analyzed the CNV status of 41,321 subjects (2,591 bipolar disorder cases and 8,842 healthy controls) and identified 3 independent CNV loci were associated with bipolar disorder: duplications at 1q21.1, deletions at 3q29 and duplications at 16p11.2. We collected this result and identified genes that were affected by these CNVs. More details about this data can be found in the original publicatioin (Green EK, Rees E, Walters JT, et al. 2016. Copy number variation in bipolar disorder. Molecular Psychiatry 2016; 21(1):89-93. PMID: 25560756).