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Table 1 Selected case-specific copy number variation loci

From: Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder

Locus Position (start–end) Gene Gain_case Loss_case Gain_control Loss_control
1p36.21 13377035–13538299 PRAMEF8,PRAMEF9,PRAMEF13,PRAMEF19,PRAMEF16,PRAMEF20 6 0 0 0
1p36.13 17262235–17295200 CROCC 4 0 0 0
1q25.1 174802140–174802829 RABGAP1L 0 4 0 0
2p11.2-p11.1 91801473–92136779 LOC654342,Mir_544,GGT8P,ACTR3BP2 7 0 0 0
3p12.3 75639495–75930920 MIR1324,FLJ20518,LOC401074,ZNF717,MIR4273 10 0 0 0
3q22.1 129806912–129914958 ALG1L2, FAM86HP 27 1 0 0
4p16.1 9486075–9744591 MIR548I2,AB059369 8 1 0 0
4p16.3 3885796–4190560 DQ584669,FAM86EP,BC042823,OTOP1 14 0 0 0
4q13.2 69371991–69410211 UGT2B15, UGT2B17 0 5 0 0
6q26 162187125–162680305 PARK2 1 3 2 0
8p23.1 12542721–12587390 LONRF1,MIR3926-1,MIR3926-2 5 0 0 0
9q13 68176154–68683835 AK308561,BC080605,LOC642236 17 0 0 0
12p13.31 8378239–8536600 LINC00937, FAM86FP, FAM90A1 5 0 0 0
14q11.2 24429298–24513905 DHRS4,DHRS4L2,DHRS4L1 1 11 5 10
19q13.42 55360538–56717229 >60 genes 4 0 0 0
21q11.2 14456404–14594223 ANKRD30BP2 8 1 0 0
22q11.23 24396802–24404830 GSTTP2 0 4 0 0