Figure 1
Figure 1. LOH 4q24 mapping and TET2 sequencing. (A) Topographical map illustrating overlapping regions of UPD4q24 (purple bars) and del4q24 (orange bars) in patients with myeloid malignancies. A minimally affected region on 4q24 (0.35 Mb), containing TET2 and PPA2, was identified in 18 of 398 patients studied (* indicates that some patients' DNA was not available for mutational screening; n = 3). (B) Representative examples of SNP-A karyograms (CNAG version 3.0) of chromosome 4 of both whole bone marrow cells and paired CD3+ lymphocytes in 2 patients, demonstrating the somatic nature of acquired LOH4q24 and TET2 mutations, which are shown in corresponding ferrograms in the right portion of the figure. SNP-A karyograms: rows a and b correspond to the copy number as measured by the intensity of individual hybridization signals; row c represents frequency of heterozygous calls; and row d indicates the allelic imbalance with parental allele copy numbers.

LOH 4q24 mapping and TET2 sequencing. (A) Topographical map illustrating overlapping regions of UPD4q24 (purple bars) and del4q24 (orange bars) in patients with myeloid malignancies. A minimally affected region on 4q24 (0.35 Mb), containing TET2 and PPA2, was identified in 18 of 398 patients studied (* indicates that some patients' DNA was not available for mutational screening; n = 3). (B) Representative examples of SNP-A karyograms (CNAG version 3.0) of chromosome 4 of both whole bone marrow cells and paired CD3+ lymphocytes in 2 patients, demonstrating the somatic nature of acquired LOH4q24 and TET2 mutations, which are shown in corresponding ferrograms in the right portion of the figure. SNP-A karyograms: rows a and b correspond to the copy number as measured by the intensity of individual hybridization signals; row c represents frequency of heterozygous calls; and row d indicates the allelic imbalance with parental allele copy numbers.

Close Modal

or Create an Account

Close Modal
Close Modal