[18F4-18F4];[19C1-19C1];
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.
18F4;19C1
Homozygous viable.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-SZ-3084 and P{RS3}CB-5193-3.