CASES WITH HETEROMORPHISMS
- Chromosome 10 -

 

      
 

Heterochromatic

- centromeric


- other heterochromatic variants

Euchromatic

- euchromatic deletions


- euchromatic amplifications

 
      

 


References

Heterochromatic

(peri)centomeric variants

 
  case no. (molecular) cytogenetic result
clinical symptoms reference  
  10-
cen+/

1-1 to few
10cen+
D10Z1
none {1 pages 68-69}  
  10-
cen-/

1-1 to few
10cen-
D10Z1
none {1 pages 68-69}  
  10-
inv/

1-1 to few
inv(10)(p11.2q21.2) none {1 pages 68-69}  
                 

other heterochromatic variants

 
  case no. (molecular) cytogenetic result clinical symptoms reference  
  10-
HHM-acro/

1-1
der(10)t(10;acro)(q26.3;p11.2) none {1; 26}  
                 

References

Euchromatic

Euchromatic deletions

 
  case no. (molecular) cytogenetic result clinical symptoms reference  
  10-EHM-
del
q11.2q11.23/

1-1
del(10)(q11.2q11.23) none {1}  
  10-EHM-
del
q11.2q21.2/

1-1
del(10)(q11.2q21.2) none {1}  
  10-EHM-
del
q22.3q23.31/

1-1
del(10)(q22.3q23.31) mild to moderate {1}  
  10-EHM-
del
q26.13qter/

1-1 to 1-2
del(10)(q26.13) none
mild to moderate
{1; 68; 77}  
  10-EHM-
del
q26.13qter/

2-1 to few
del(10)(q26.13)
reduction of signal size
none {77}  
                 

Euchromatic duplications

 
  case no. (molecular) cytogenetic result clinical symptoms reference  
  10-EHM-
dup
p15p14
/

1-1
dup(10)(p15p14) mild to moderate {1}  
  10-EHM-
dup
p15p13
/

1-1
dup(10)(p15p13) mild to moderate {1}  
  10-EHM-
dup
p14p13
/

1-1
dup(10)(p14p13) none {1}  
  10-EHM-
dup p11.22q11.22/

1-1 to few
sSMC(10) none
{sSMC
page
}
 
  10-EHM-
dup
q26.3qter
/

1-1
dup(10)(q26.3qter)

none in father of affectced child

{68}