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Table 1 Frequency of chromosomal polymorphism variation

From: Impact of parental chromosomal polymorphisms on the incidence of congenital anomalies and perinatal complications in a cohort of newborns conceived after ICSI + PGT-A

Karyotype

 

No. of males with Heteromorphisms

(n = 1,319)

Freq

(%)

No. of females with Heteromorphisms

(n = 1,319)

Freq

(%)

Total

 

29

 

37

 

Chromosomes 1, 9, 16

 

11

37.9%

22

59.5%

1q + 

4

13.8%

1

2.7%

9q + 

2

6.9%

3

8.1%

9q-

0

 

1

2.7%

9cenh + 

0

 

1

2.7%

Inv(9)

5

17.2%

11

29.7%

16q + 

0

 

5

13.5%

Acrocentric chromosome (D/G group)

 

12

41.4%

12

32.4%

13 ps + /pss

1

3.4%

1

2.7%

14 ps + /pss

3

10.3%

4

10.8%

14pstk + 

1

3.4%

0

 

15 ps + /pss

2

6.9%

0

 

15cenh + 

1

3.4%

0

 

21 ps + /pss

2

6.9%

1

2.7%

22 ps + /pss

1

3.4%

6

16.2%

22pstk + 

1

3.4%

0

 

Y chromosome variation

 

4

13.8%

0

 

Yq + 

3

10.3%

  

Yqs + 

1

3.4%

  

Multiple variations

 

2

6.9%

3

8.1%

9qh + ,21 ps + 

1

3.4%

1

2.7%

21 ps + ,22 ps + 

1

3.4%

0

 

inv(9)(p12q12),21 ps + 

0

 

1

2.7%

14pstk + ,14pstk + 

0

 

1

2.7%