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Table 1 Comparison between results of the current study and results from other studies

From: Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins

 

Findings from different studies

Overlapped CNVRs of this study

 

Study

Breed

Sample

Count

Total length (Mb)

Count

Percentage of count

Total length (Mb)

Percentage of length

CGH-based Studies

Fadista et al. [25]a

4

20

266

16.6

27

9.7%

1.71

8.7%

Liu et al. [24]b

17

90

177

28.1

16

5.8%

1.58

8.1%

SNP-based Studies

Hou et al. [26]

21

521

682

139.8

55

19.8%

5.35

27.3%

Bae et al. [23]

1

265

368

63.1

35

12.6%

2.00

10.2%

Hou et al. [58]

1

472

811

141.8

51

18.3%

3.41

17.4%

Jiang et al. [60]

1

2047

101

23.8

14

5.0%

2.50

12.8%

Hou et al. [55]

27

674

3346

142.7

119

42.8%

7.59

38.7%

Resequencing-based Studies

Bickhart et al. [8]

3

5

1265

55.6

19

6.8%

0.855

4.4%

Zhan et al. [5]

1

1

520

3.6

13

4.7%

0.253

1.3%

Stothard et al. [4]

2

2

790

3.3

14

5.0%

0.380

1.9%

This study

 

278

19.6

 
  1. Based on Btau4.0 bovine genome assembly.
  2. a: CNVRs on Chr Un and mitochondrial sequence are excluded;
  3. b: CNVRs on Chr Un are excluded.