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Table 4 Summary of CNVR per chromosome for all panels

From: Detection of copy number variations in brown and white layers based on genotyping panels with different densities

Chr

Chr length (Mb)

Merged CNVRa

Merged CNVR N ≥ 2b

Intersected CNVR N ≥ 2c

Number

Number

Fraction of chr coveredd

Number

Fraction of chr coveredd

Genese

1

195.3

544

234

0.370

378

0.111

0.050

2

148.8

435

186

0.322

264

0.101

0.036

3

110.4

317

138

0.321

192

0.089

0.036

4

90.2

258

113

0.389

172

0.103

0.042

5

59.6

184

85

0.394

136

0.145

0.076

6

35.0

135

59

0.362

87

0.107

0.064

7

36.2

86

46

0.522

96

0.178

0.100

8

28.8

79

38

0.429

68

0.128

0.061

9

23.4

63

37

0.497

67

0.192

0.091

10

19.9

72

38

0.452

63

0.148

0.078

11

19.4

55

27

0.432

51

0.112

0.061

12

19.9

54

27

0.528

58

0.171

0.111

13

17.7

61

26

0.480

43

0.183

0.084

14

15.1

46

26

0.457

47

0.164

0.094

15

12.7

22

18

0.760

55

0.258

0.141

16

0.5

1

1

0.979

2

0.923

0.564

17

10.4

26

16

0.677

44

0.210

0.102

18

11.2

30

18

0.523

39

0.158

0.084

19

10.0

17

12

0.786

40

0.186

0.127

20

14.3

43

20

0.495

39

0.175

0.085

21

6.8

35

17

0.456

30

0.156

0.078

22

4.1

8

5

0.664

17

0.199

0.068

23

5.7

21

13

0.593

28

0.164

0.091

24

6.3

24

12

0.626

28

0.172

0.111

25

2.2

4

5

0.701

16

0.203

0.092

26

5.3

25

16

0.485

22

0.167

0.083

27

5.2

24

18

0.698

27

0.255

0.183

28

4.7

18

13

0.622

30

0.243

0.143

  1. Chr chromosome
  2. aMerged CNVR = All CNVR merged across all lines; 2687 CNVR in total
  3. bCommon CNVR N ≥ 2 = Merged CNVR observed in at least two individuals within a line, merged across all lines; 1264 CNVR in total
  4. cCommon intersected CNVR N ≥ 2 = Intersected CNVR observed in at least two individuals within a line, merged across all lines; 2139 CNVRs in total
  5. dFraction of chromosome covered with CNVR
  6. eFraction of CNVR overlapping with genes