[85D19-85D19];[85F8-85F8];
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.
85D19;85F8
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Flies heterozygous for the deletion show a Minute bristle phenotype.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}ps10615&P{PZ}Ras85D06677 and P{EP}CG9393EP3122 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}s2681 and P{EP}Fmr1EP3517&P{PZ}tws02414