Breast cancer is characterised by a number of genetic aberrations. Our purp
ose was to use comparative genomic hybridisation (CGH) to screen breast car
cinomas for copy number changes: 44 ductal and 8 lobular carcinomas were st
udied and a large number of genetic aberrations identified. Many of these s
howed similarity to previous CGH results, however, a number of loci not pre
viously shown to have undergone frequent change were identified. This inclu
ded copy number gains affecting chromosomes 1p, 4q, 5q, 6q and 13q, Further
more, we have identified 2 regions of copy number change, the gain on 5p an
d deletion of 16q, which correlated with lobular carcinomas. Our results hi
ghlight several areas of the genome that may be important in the molecular
genetics of breast cancer. Int. J, Cancer 86:494-500, 2000, (C) 2000 Wiley-
Liss, Inc.