Acute myeloid leukemia (AML) is a group of highly heterogeneous hematopoietic malignancies, often associated with acquired chromosomal abnormalities, the most common of which is chromosomal translocation. Chromosomal inversion of inv16 (p13q22) or translocation t(16;16) (p13; q22) found in myeloid leukemia (AML-M4) cells with eosinophilia, resulting in the MYH11 gene located at 16p13. The CBFB gene located at 16q22 is recombined to form a CBFB/MYH11 gene fusion. The detection rate of CBFB/MYH11 gene fusion in myeloid leukemia is about 7%. Since the CBFB/MYH11 gene fusion is only found in AML, according to the WHO leukemia diagnostic criteria, AML can be diagnosed by detecting the CBFB/MYH11 gene fusion.