The present invention relates to DNA sequences from regions of copy number change on chromosome 20. The sequences can be used in hybridization methods for the identification of chromosomal abnormalities associated with various diseases.
STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
This invention was made with Government support under Grant Nos. DE-AC-03-76SF00098 & DE-AC-03-79SF00098, awarded by the Dept. of Energy; CA58207, awarded by the National Institutes of Health; 94-05-0021, awarded by the National Inst. Standards Tech. The Government has certain rights in this invention.