Table 4.
Total Variant Frequency |
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0.05a |
0.01b |
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No. Included | S | H | C | S | H | C |
0 | 0.05 | 0.40 | 0.86 | 0.05 | 0.39 | 0.83 |
5 | 0.04 | 0.30 | 0.70 | 0.04 | 0.29 | 0.68 |
10 | 0.03 | 0.23 | 0.55 | 0.03 | 0.23 | 0.55 |
20 | 0.03 | 0.16 | 0.33 | 0.02 | 0.15 | 0.36 |
No. Excluded | S | H | C | S | H | C |
2 | 0.05 | 0.31 | 0.72 | 0.05 | 0.30 | 0.69 |
4 | 0.05 | 0.21 | 0.52 | 0.04 | 0.20 | 0.50 |
6 | 0.04 | 0.12 | 0.28 | 0.04 | 0.12 | 0.27 |
8 | 0.03 | 0.05 | 0.08 | 0.03 | 0.05 | 0.08 |
The effect of including noncausal variants and excluding causal variants on the power of the single-marker test (S), Hotelling's T2 test (H), and the collapsing method (C) when there are ten rare causal variants in a gene, with a total variant frequency of either 0.05 or 0.01. In the upper section of the table, also included in the analysis are 5, 10, and 20 rare noncausal variants, with the same allele frequencies as the causal variants. In the lower section of the table, 2, 4, 6, and 8 causal variants are excluded from the analysis.
Sample size of 250 cases and 250 controls.
Sample size of 1000 cases and 1000 controls.