Table 1 CNVs of tandem sequence blocks.

From: An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome

Sample ID

LCR22.2

LCR22.4

K3

L9

B22

L21

K3

L9

B22

M12

I18

Controls

C1

5\7

5\6

2\3

1\2

2\3

2\2

1\2

2\2

2\2

C2

7\9

5\10 *

3\5 *

1\2

2\2

2\2

1\2

2\2

2\3

C3

3\5

3\5

1\2

1\2

1\2

1\2

1\1

2\2

2\2

C4

3\5

3\5

2\3

1\1

2\2

2\2

1\1

2\2

2\2

C5

3\3

2\5

2\4

1\2

1\2

1\2

2\2

2\2

2\2

C6

3\5

2\4

1\2

1\1

1\2

2\2

1\2

2\2

2\2

Normal range **

3–9

2–6

1–4

1–2

1–3

1–2

1–2

2–2

2–3

DGS/VCFS fathers ***

DG2F

2\2

3\6

2\3

1\2

2\2

2\3

1\2

2\2

2\2

DG5F

5\8

8\8

2\3

1\2

2\2

2\3

1\2

2\2

2\2

  1. *Outlier. **Ranges established with the lowest and the highest values in control individuals excluding outliers. ***DGS/VCFS fathers-of-origin with increased number of 22q11.2 sperm deletions (Vergés et al.13). The two haplotypes for each individual are separated by a backslash. Bold numbers indicate CNVs out of the normal range.
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