64F2-64F5;65D1-65D3;h53R-h58
64E;65C-65D
64F2-64F5;65D1-65D3;h53R-h58
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
The Df(3L)v65c chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by one or more nonsuppressing deficiencies.
"64F2--5;65D1--3;h53R--h58" was stated as revision. "deficient_inversion ; SO:1000171" was stated as revision. Noncomplementation with Df(3L)v65c may be due to position effect variegation of wild type alleles on the deletion chromosome rather than deletion of genomic sequences.
All limits from polytene analysis (FBrf0080317)