Copy-number-variation and copy-number-alteration region detection by cumulative plots

Abstract

Background: Regions with copy number variations (in germline cells) or copy number alteration (in somatic cells) are of great interest for human disease gene mapping and cancer studies. They represent a new type of mutation and are larger-scaled than the single nucleotide polymorphisms. Using genotyping microarray for copy number variation detection has become standard, and there is a need for improving analysis methods. Results: We apply the cumulative plot to the detection of regions with copy number variation/alteration, on samples taken from a chronic lymphocytic leukemia patient. Two sets of whole-genome genotyping of 317 k single nucleotide polymorphisms, one from the normal cell and another from the cancer cell, are analyzed. We demonstrate the utility of cumulative plot in detecting a 9 Mb (9 × 106 bases) hemizygous deletion and 1 Mb homozygous deletion on chromosome 13. We also show the possibility to detect smaller copy number variation/ alteration regions below the 100 kb range. Conclusion: As a graphic tool, the cumulative plot is an intuitive and a scale-free (window-less) way for detecting copy number variation/ alteration regions, especially when such regions are small. © 2009 Li et al; licensee BioMed Central Ltd.