Genetic copy number variants in sib pairs both affected with schizophrenia

Table 2 The highly recurrent CNVs in schizophrenic subjects

^a The aberration scores (n) are calculated by using the Agilent aberration detection method: no change is defined as n = 0, loss as n < -1, and gain as n > 1. Bold type indicates CNS-related genes. Description and GenBank accession no.: Protein kinase, AMP-activated, gamma 2 non-catalytic subunit (PRKAG2 , NM_001040633), Kruppel-like factor 5 (KLF4, NM_001730); UBA domain containing 1 (UBADC1, NM_016172); lipocalin 6 (LCN6, NM_198946); lipocalin 8 (LCN8, NM_178469); chromosome 9 open reading frame 37 (C9orf37, NM_032937); collagen, type XIII, alpha 1(COL13A1, NM_001130103); Rh family, C glycoprotein (RHCG, NM_016321); septin 9 (SEPT9, NM_001113496); poliovirus receptor (PVR, NM_006505); and chromosome 21 open reading frame 57 (C21orf57, NM_058181).

ISSN: 1423-0127