[55C2-55C2];[56C4-56C4];
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.
55C2;56C4
Inferred to overlap with: Df(2R)BSC335.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by 3-step PCR confirmation as shown in 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}sbb04525&P{EP}EP1081EP1081 and P{lacW}l(2)08770k04808 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}ena02029&P{lacW}corak08713 and P{lacW}htsk06121