This report describes the development and validation of quantitative micros
atellite analysis (QuMA) for rapid measurement of relative DNA sequence cop
y number. In QuMA, the copy number of a test locus relative to a pooled ref
erence is assessed using quantitative, real-time PCR amplification of loci
carrying simple sequence repeats, Use of simple sequence repeats is advanta
geous because of the large numbers that are mapped precisely, In addition,
all markers are informative because QuMA does not require that they be poly
morphic. The utility of QuMA is demonstrated in assessment of the extent of
deletions of chromosome 2 in leukemias arising in radiation-sensitive inbr
ed SJL mice and in analysis of the association of increased copy number of
the putative oncogene ZNF217 with reduced survival duration in ovarian canc
er patients.