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Table 2 CNV detected on autosomes of 12 pairs of samples

From: Identifying potential biomarkers of nonalcoholic fatty liver disease via genome-wide analysis of copy number variation

Sample number

Gains (CNV-containing genes)

Losses (CNV-containing genes)

Range of CNV (kb–Mb)

Total length of CNV (Mb)

Percentage of genome length (%)

Number of genes

Pair 1

40 (26)

3 (3)

15.60–2.35

9.91

0.17

68

Pair 2

6 (4)

38 (32)

7.46–1.93

4.72

0.11

62

Pair 3

5 (4)

87 (52)

7.46–0.46

8.79

0.19

88

Pair 4

9 (8)

6 (5)

5.70–1.17

2.68

0.05

40

Pair 5

1 (1)

39 (31)

8.53–2.23

7.57

3.16

50

Pair 6

4 (4)

4 (2)

27.55–2.08

3.50

0.57

22

Pair 7

2 (2)

4 (4)

20.67–0.46

1.03

0.60

11

Pair 8

12 (1)

5 (3)

10.03–2.35

5.73

0.10

65

Pair 9

6 (6)

46 (34)

7.46–2.03

7.23

0.12

86

Pair 10

8 (7)

7 (6)

9.34–2.13

5.49

0.09

52

Pair 11

13 (11)

16 (14)

17.57–0.85

5.38

0.09

88

Pair 12

11 (10)

9 (6)

13.20–2.27

7.24

0.12

82