18E1-18E2;20E-20F
18E1-18E2;20
Cdc42 << bk1 << sw << su(f) << bk2
Weak second site non-complementing phenotype with zipEbr and zipmhc-c6.1 : malformed phenotype penetrance 10-24%.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Lefevre.
Limits of break 1 from polytene analysis (FBrf0034402) Left limit of break 2 from inclusion of su(f) (FBrf0034402) Right limit of break 2 from polytene analysis (FBrf0034402)