Figure 5
Figure 5. Frequency plot of all CLL samples versus normal CNV database. The frequency plot for 58 CLL samples is shown in blue and that of 500 “normal” (ie, disease-free) individuals is shown in red. The red frequency plot shows CNVs in the human genome and was used to eliminate any CNVs in our data exposed through copy-neutral LOH (ie, regions in which CNVs overlap with lesions observed in CLL). Most lesions observed in CLL are deletions and trisomy 12. Regions of interest are marked with arrows.

Frequency plot of all CLL samples versus normal CNV database. The frequency plot for 58 CLL samples is shown in blue and that of 500 “normal” (ie, disease-free) individuals is shown in red. The red frequency plot shows CNVs in the human genome and was used to eliminate any CNVs in our data exposed through copy-neutral LOH (ie, regions in which CNVs overlap with lesions observed in CLL). Most lesions observed in CLL are deletions and trisomy 12. Regions of interest are marked with arrows.

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