Table 1.

Genetic Map and Marker Statistics

Marker Map position (cM) H Alleles observed[ii] Alleles analyzed[iii]
S1030.00.7085
S1170.50.87158
S9065.10.78126
S1939.10.72134
S88910.00.82198
S48211.80.6994
S84914.80.69175
S90518.60.64114
S89220.60.86128
S84620.60.73105
S11522.10.6474
S85125.50.76146
S91726.20.87168
S89430.40.83127
S18932.40.69106
S89837.30.74185
S11442.70.83117
S91248.20.83127
S47748.90.74115
S87452.10.79166
S19552.70.85167
S90953.40.70165
S10758.10.84156
S17059.60.80178
S9662.40.82137
S11965.70.80106
S48165.90.83138
S83666.90.83127
S88867.70.90208
S88668.10.86107
S19769.10.75116
S17870.20.78117
S86671.80.85198
S19674.50.79234
S85776.30.84138
S48079.20.75116
S84080.20.80187
S21180.20.65135
S12083.20.83187
S10085.80.74125
S10287.70.4454
S17196.10.80136
S17399.20.73137

[i] H, Heterozygosity.

[ii] Number of alleles observed in an average of 5114 individuals per marker, typed as part of the FUSION study.

[iii] Number analyzed when alleles with a frequency below 5% are pooled.