t(14;14)(q11;q32)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An intrachromosomal translocation involving breakpoints within the q11 and the q32 bands on the long arm of chromosome 14. This translocation may be associated with ATG2B-SLC22A17 fusion gene expression and solid tumors, aberrant expression of the CEBPE gene and acute lymphoblastic leukemia/lymphoblastic lymphoma or aberrant expression of TCL1A and hematologic disorders.