Figure 1
Figure 1. Single nucleotide polymorphism 6.0 arrays result in a patient with del 5q in the setting of the 5q− syndrome. There is loss of heterozygosity (LOH) and reduction in copy number in the q arm of chromosome 5. These changes represent a deletion in that region of chromosome 5 (blue box). In an attempt to identify the putative genetic defects that causes 5q− syndrome, several investigators defined different commonly deleted regions (CDRs) in chromosome 5. Shown here are the CDRs from Boultwood et al4 and the putative genes of interest.

Single nucleotide polymorphism 6.0 arrays result in a patient with del 5q in the setting of the 5q− syndrome. There is loss of heterozygosity (LOH) and reduction in copy number in the q arm of chromosome 5. These changes represent a deletion in that region of chromosome 5 (blue box). In an attempt to identify the putative genetic defects that causes 5q− syndrome, several investigators defined different commonly deleted regions (CDRs) in chromosome 5. Shown here are the CDRs from Boultwood et al4 and the putative genes of interest.

Close Modal

or Create an Account

Close Modal
Close Modal