Chromosomal abnormalities revealed by SKY in TCL1+/wtMIFwt/wt (n = 3) and TCL1+/wtMIF−/− (n = 4) mice
Genotype . | Assessment by SKY . |
---|---|
TCL1+/wtMIFwt/wt | |
1 | 41,XY,+15 [6]/ 42–43,XY,+10,+Del(15) [cp5]/ 40,XY [4] |
2 | 80 < 4n > ,XXYY [8]/ 40,XY [7] |
3 | 41,XY,+15 [14] |
TCL1+/wtMIF−/− | |
1 | 40,X,-X,+15 [2]/ 41,XX,+15 [1]/ 40,XX [8] |
2 | 71∼75,XXY,-Y,Der(1)T(1;?10),Der(4)T(4;?),Der(15)T(7;15),mar [cp9] /40,XY [4]/ 80 < 4n > ,XXYY [2] |
3 | 40,XY [10] |
4 | 40,X,-Y,+15 [9]/ 41,XY,+15 [5] |
Genotype . | Assessment by SKY . |
---|---|
TCL1+/wtMIFwt/wt | |
1 | 41,XY,+15 [6]/ 42–43,XY,+10,+Del(15) [cp5]/ 40,XY [4] |
2 | 80 < 4n > ,XXYY [8]/ 40,XY [7] |
3 | 41,XY,+15 [14] |
TCL1+/wtMIF−/− | |
1 | 40,X,-X,+15 [2]/ 41,XX,+15 [1]/ 40,XX [8] |
2 | 71∼75,XXY,-Y,Der(1)T(1;?10),Der(4)T(4;?),Der(15)T(7;15),mar [cp9] /40,XY [4]/ 80 < 4n > ,XXYY [2] |
3 | 40,XY [10] |
4 | 40,X,-Y,+15 [9]/ 41,XY,+15 [5] |