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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