Figure 5.
Association of SNP array results with immunophenotype and oncogenetics. (A-C) Box plots showing the number of genomic imbalances per sample according to immunophenotypic subgroups: immature, αβ lineage and mature TCR γδ (A), in ETP and non-ETP subgroups (B), and according to oncogenetics subgroups: SIL-TAL1, TLX1, TLX3, HOXA9 overexpressing, and negative subgroups (C). (D-E) Venn diagram indicating the recurrent genomic imbalances with a significantly higher incidence between the immunophenotypic subgroups (D) and ETP vs non-ETP subgroups (E) (P < .01). (F) Bar plots indicating the incidence of recurrent genomic imbalances according to oncogenetic subgroups. ∗P < .01.

Association of SNP array results with immunophenotype and oncogenetics. (A-C) Box plots showing the number of genomic imbalances per sample according to immunophenotypic subgroups: immature, αβ lineage and mature TCR γδ (A), in ETP and non-ETP subgroups (B), and according to oncogenetics subgroups: SIL-TAL1, TLX1, TLX3, HOXA9 overexpressing, and negative subgroups (C). (D-E) Venn diagram indicating the recurrent genomic imbalances with a significantly higher incidence between the immunophenotypic subgroups (D) and ETP vs non-ETP subgroups (E) (P < .01). (F) Bar plots indicating the incidence of recurrent genomic imbalances according to oncogenetic subgroups. ∗P < .01.

or Create an Account

Close Modal
Close Modal