t(7;11)(p15;p15)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A chromosomal translocation involving breakpoints within the p15 band on the short arm of chromosome 7 and the p15 band on the short arm of chromosome 11. This rearrangement is associated with expression of NUP98-HOXA9, NUP98-HOXA11 or NUP98-HOXA13 fusion genes and myeloid neoplasms.