[22F4-22F4];[23B8-23B8];
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.
22F4;23B8
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Lethal over SM6a.
Viable in combination with Dp(2;2)EDP5.
Flies heterozygous for the deletion show a Minute bristle phenotype.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}dpp10638 and P{EP}EP832 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}oho23B03575 and P{PZ}lilli00632