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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