Table 5.

Cytogenetic abnormalities encountered in HOXB6- and HOXA9-induced AMLs


Vector and ID

Karyotype
HOXB6  
    29847   40,XY,del(2)(BE4)[6]/41,idem,+del(2)(BE4)[4]  
    29848   40,XX,del(2)(C1H3)/[9]/40,XX,del(2)(C2F3)[1]  
    29849   40,XX[10]  
    29850   40,XY[10]  
    29851   40,XX[10]  
HOXA9  
    29495   40,XY[10]  
    29497   41,XX,+X,del(2)(A2H2)[10]  
    29498   40,XX[10]  
    29779   40,XY[10]  
    28299   40,XY,del(2)(DH4)[9]/39, idem, -10, -17, +dic mar[1]  
    28298
 
40,XY,del(2)(DH4)[10]
 

Vector and ID

Karyotype
HOXB6  
    29847   40,XY,del(2)(BE4)[6]/41,idem,+del(2)(BE4)[4]  
    29848   40,XX,del(2)(C1H3)/[9]/40,XX,del(2)(C2F3)[1]  
    29849   40,XX[10]  
    29850   40,XY[10]  
    29851   40,XX[10]  
HOXA9  
    29495   40,XY[10]  
    29497   41,XX,+X,del(2)(A2H2)[10]  
    29498   40,XX[10]  
    29779   40,XY[10]  
    28299   40,XY,del(2)(DH4)[9]/39, idem, -10, -17, +dic mar[1]  
    28298
 
40,XY,del(2)(DH4)[10]
 

Spectral karyotyping performed on 5 HOXB6- and 5 HOXA9-induced AMLs reveals recurrent deletions of chromosome 2 in 3 HOXA9-induced and 2 HOXB6-induced AMLs.

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