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. 2020 Feb 24;4(4):696–705. doi: 10.1182/bloodadvances.2019000492

Table 3.

Additional cytogenetic abnormalities in patients with previously untreated CBF AML

UPN Sex Secondary chromosome abnormality(s)
Patients with t(8;21)
1 Female ‒X
5 Female ‒X
48 Female ‒X
58 Female ‒X
6 Male ‒Y
7 Male ‒Y
10 Male ‒Y
23 Male ‒Y
4 Male del(9)(q13q22)
12 Female del(9)(q13q22)
47 Male del(9)(q31q33)
13 Female ‒X,del(9)(q13q22)
16 Male ‒Y,del(9)(q12q22)
45 Male ‒Y,del(9)(q13q22)
34 Male +4
43 Female add(5)(q33)
27 Male +8/del(12)(p12)
11 Female Tetraploid clone with t(8;21)x2
Patients with inv(16) or t(16;16)
20 Male +8
46 Female +8
8 Female +8/add(17)(q23)
14 Male +6,+8,+19,+20,+21,+22
37 Female t(11;20)(p15;q11.2)/+8,t(11;20)(p15;q11.2)
52 Male +21/+6,+8,+13,+21/+13,t(13;16)(q14;q24),+20,+21/+13,+21
56 Female del(7)(q32q36)/+8,+14,+14,+21/+22
42 Male +6
28 Female +9
22 Male +22
33 Female del(16)(q22q22)/del(16)(q22q22),+22
36 Female +9,+14,+22
30 Male del(5)(q15q34)
29 Female der(1)inv(1)(p13.3q11)del(1)(q41q43),t(4;6)(q34;p12),add(7)(q34), ‒10,+r,+mar