[88D1-88D1];[88E2-88E2];
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
88D1;88E2
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}put10460 and P{EP}CG33967EP666 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG33967EP666 and P{lacW}Hsc70-4L3929