[37B1-37B1];[37C5-37C5];
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.
37B1;37C5
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Lethal in combination with Df(2L)BSC332.
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{EP}CG10413EP2164 and P{lacW}l(2)37Dbk16106&P{lacW}Catsupk05424 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Ddck02104 and P{lacW}bratk06028&P{lacW}l(2)k09613k09613