Table 3.

A list of rare discordant CNVs, including: the positions (GRCh38); length; type (DEL deletion, DUP duplication); the carrier sample ID; their phenotype (SAD schizoaffective disorder, SCZ schizophrenia); if they are annotated as pathogenic; and the overlapping genes from the BDgene and SZDB databases (full list in Supplementary Tables 8, 9).

Chr	Start	End	Length	Type	Sample	Pheno	Path	BDgene	SZDB
chr3	195940567	197638156	1,697,589	DUP	T17_A	BD	Y	BDH1; DLG1	20 Genes
chr10	92847856	92849207	1351	DEL	T02_A	SAD			EXOC6
chr12	120201498	120204299	2801	DEL	T16_A	BD
chr19	11261852	11262999	1147	DEL	T01_A1	SCZ