t(11;17)(q13;q11)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A chromosomal translocation involving breakpoints within the q13 band on the long arm of chromosome 11 and the q11 band on the long arm of chromosome 17. This translocation may be associated with the expression of various fusion genes (including ANO1-ABHD15, FAM168A-SLC13A2, PPP6R3-SSH2 and TAOK1-ACER3) and solid tumors.