[56D5-56D5];[56D5-56D5];
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.
56D5;56D5
Homozygous lethal. Muscle attachment sites are unaffected in mutant embryos.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS3}htsUM-8250-3 and P{RS5}Fak56D5-SZ-3124.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}htsk06121 and P{lacW}l(2)k00705k00705&P{lacW}mei-W68k05603