Figure 3From: Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A Overview of all mutations, focal deletions, 6q deletions, and TCR rearrangements identified by large-scale sequencing, SNP array, and FISH analyses of the pediatric T-ALL cohort.Back to article page