Short tandem repeat (STR) markers are currently used to define loss of hete
rozygosity (LOH) of genes and chromosomes in tumors. Chromosome 6 and chrom
osome 15 STR markers are applied to define loss of HLA and related genes (e
.g. TAP and beta(2)m) The number of STR identified in the HLA region is sti
ll increasing. In this study, seven representative STR markers covering the
6p/6q arms of chromosome 6 including the HLA region and two for chromosome
15 flanking the beta(2)m gene, were selected as minimally required for rel
iable LOH studies. A multiplex polymerase chain reaction (PCR) strategy is
proposed when small number of cells are available in microdissected tumor s
amples.