Table 2

CNVs abnormalities of possible significance in cases with both schizophrenia and epilepsy.

NIMH ID

Sex

Chr.

Start

Size (bp)

CNV

Genes

Validation

DGV


140-2082-001

M

8p11.21

42582092

7817

Loss

CHRNB3

Cus2

None

143-2447-001

M

9p24.2

4409405

134869

Loss

SLC1A1

Cus2

2 overlap

144-1472-001

M

11q14.1

84188228

482969

Loss

DLG2

Cus2

None

147-2093-001

M

12q14.3

67049795

150443

Loss

GRIP1

Cus4

None

144-1461-001

M

20p13

3897943

1039259

Loss

12

Cat

None


Abbreviations: As in Table 1.

Stewart et al. BMC Medical Genetics 2011 12:154   doi:10.1186/1471-2350-12-154

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