[27F4-27F4];[28C4-28C4];
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.
27F4;28C4
Inferred to overlap with: Df(2L)BSC233.
Fails to complement Df(2L)BSC189.
Inferred to overlap with: Df(2L)BSC189.
Inferred to overlap with: Df(2L)BSC190.
Lethal in combination with Df(2L)BSC190.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}wg02657 and P{EP}EP787EP787 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP2419EP2419&P{EP}EP575 and P{PZ}l(2)rL220rL220