TABLE 1

Stocks used for deficiency complementation mapping

Chromosome 2Chromosome 3
QTLGenotypeCytogenetic locationQTLGenotypeCytogenetic location
57C–57FDf(2R)CX149C1–4; 50C23–D272A–85FDf(3L)vin768C8–11; 69B4–5
Df(2R)L4850F6–9; 51B3Df(3L)iro-269B1–5; 69D1–6
Df(2R)trix51A1–2; 51B6In(3LR)C19069F3–4; 70C3–4
Df(2R)0307251A5; 51C1Df(3L)fz-CAL570C2–6; 70E1
Df(2R)Jp151D3–8; 52F5–9Df(3L)Brd670E; 71F
Df(2R)vg89e8852B3–C1; 53E2–F2Df(3L)brm1171F1–4; 72D1–10
Df(2R)Jp652E3–5; 52FDf(3L)st-F1372C1–D1; 73A3–4
Df(2R)Jp852F5–9; 52F10–53A1Df(3L)81k1973A3; 74F
Df(2R)Pcl7B54E8–F1; 55B9–C1Df(3L)W1075A6–7; 75C1–2
Df(2R)PC455A; 55FDf(3L)VW376A3; 76B2
Df(2R)P3455E2–4; 56C1–11Df(3L)kto276B1–2; 76D5
Df(2R)01756F5; 56F15Df(3L)XS-53376B4; 77B
Df(2R)min56F8–17; 56F8–17Df(3L)rdgC-co277A1; 77D1
Df(2R)AA2156F9–17; 57D11–12Df(3L)ri-79c77B–C; 77F–78A
Df(2R)D457A1–3; 57B13Df(3L)ME10777F3; 78C8–9
Df(2R)exu157A2; 57B1Df(3L)Pc-2q78C5–6; 78E3–79A1
Df(2R)Pu-D1757B4; 58BDf(3L)Delta1AK79F; 80A
Df(2R)X58-758B1–2; 58E4–10Df(3R)ME1581F3–6; 82F5–7
Df(2R)X58-1258D1–2; 59ADf(3R)3-482F3–4; 82F10–11
Df(2R)59AB59A1–3; 59B1–2Df(3R)Tp11083C1–2; 84B1–2
Df(2R)59AD59A1–3; 59D1–4Df(3R)roe84A6–B1; 84D4–D9
Df(2R)twi59C3–4; 59D1–2Df(3R)dsx284C1–3; 84E1
Df(2R)bw-S4659D8–11; 60A7Df(3R)p71284D4–6; 85B6
Df(2R)or-BR659D5–10; 60B3–8Df(3R)p-XT10385A2; 85C1–2
Df(2R)Chi[g230]60A3–7; 60B4–7Df(3R)by1085D8–12; 85E7–F1
Df(2R)Px160B8–10; 60D1–2Df(3R)by6285D11–14; 85F16
Df(2R)Px260C5–6; 60D9–10Df(3R)M-Kx186C1; 87B1–5
Df(2R)M60E60E2–3; 60E11–12Df(3R)T-3286E2–4; 87C6–7
Df(2R)ES160E6–8; 60F1–2Df(3R)ry61587B11–13; 87E8–11
Df(2R)Kr1060F1; 60F5
Df(2R)Kr1460F2; 60F5
96F–99ADf(3R)96B96A21; 96C2
Df(3R)Espl396F1; 97B1
Df(3R)Tl-P97A; 98A1–2
Df(3R)D60597E3; 98A5
Df(3R)345098E3; 99A6–8
Df(3R)Dr-rv199A1–2; 99B6–11
Df(3R)0121599A6; 99C1
Df(3R)L12799B5–6; 99E4–F1
Df(3R)B8199C8; 100F5
Df(3R)awd-KRB100C;100D