[53C9-53C9];[53F10-53F10];
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.
53C9;53F10
Lethal in combination with Df(2R)BSC382.
Lethal in combination with Df(2R)BSC433.
Inferred to overlap with: Df(2R)BSC382.
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.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}Sema-2a03021&P{PZ}Cdk405428 and P{EP}BEST:SD02913EP2148&P{lacW}Dekk09907 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k10815k10815 and P{EP}EP710