Medical Genetics Genome mutation Genome mutations are alterations in the number of intact chromosomes(called aneuploidy)arising from errors in chromosome segregation during meiosis or mitosis. Origin:missegregation of a chromosome pair during meiosis. Consequence:chromosomal aneuploidy. The most common mutations seen in humans; also common in cancer cells. This document is produced by trial version of Print2Flash.Visit www.print2flash.com for more informationThis document is produced by trial version of Print2Flash. Visit www.print2flash.com for more information