11D1;12A1
11D;12A1-12A2
11;12A1-12A2
11D-11E;12A1-12A2
[];12A1--2
11D-11E;12A1
gs(1)N41 << bk1 << l(1)11Dc << Gpt << bk2 << up
YSX.YL, Df(1)C246, In(1)EN, y M/C(1;Y)2, Df(1)gl In(1)EN, y g f B females are viable, yellow and Minute (Schalet).
Flies heterozygous for the deletion show a Minute bristle phenotype.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.
Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences and detachments.
Mutants show a moderate Minute phenotype.
Lefevre.
Left limit of break 1 from polytene analysis (citation unavailable) Right limit of break 1 from inclusion of rad (FBrf0053305) Left limit of break 2 from polytene analysis (FBrf0034402) Right limit of break 2 from polytene analysis (FBrf0086390)