Table 2.

Results of fluorescence in situ hybridization analysis

No. of Patients (%) (n = 34)
t(11;18)(q21;q21)	0 (0%)
t(14;18)(q32;q21)	1(3%)
trisomy 18*	16 (47%)
trisomy 3**	21 (62%)
trisomy 7	2 (6%)
trisomy 12	0 (0%)
MALT 1 gene amplification	1 (3%)
Normal	3 (9%)

* There were eight cases with trisomy 18 alone and eight cases with trisomy 18 and trisomy 3.

** There were eleven cases with trisomy 3 alone, eight with trisomy 3 and trisomy 18, one with t(14;18)(q32;q21), and one with MALT1 gene amplification.