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. 2016 Aug 6;32(23):3603–3610. doi: 10.1093/bioinformatics/btw500

Table 1.

Testing P-values of association between ASD and CNVs in each chromosome

Chromosome #CNVs CKAT Fisher’s exact CCRET
chr1 175 8.2e-2 3.1e-1 3.5e-2
chr2 45 1.7e-4 (*) 4.3e-4 (*) 2.4e-2
chr3 49 0 (*) 1.8e-14 (*) 1
chr4 112 8.2e-1 8.3e-1 8.6e-1
chr5 242 2.3e-2 2.3e-2 9.4e-2
chr6 17 1.2e-4 (*) 3.4e-5 (*) 1
chr7 25 1.2e-4 (*) 1.4e-4 (*) 3.1e-2
chr8 3 0.1e-1 2.5e-1 1
chr9 13 7.7e-1 7.8e-1 2.1e-1
chr10 130 4.7e-1 3.3e-1 4.2e-1
chr11 257 8.8e-1 8.0e-1 5.6e-1
chr12 3 2.7e-1 6.1e-1 1.1e-1
chr13 5 7.4e-1 1 3.2e-1
chr14 2 1.8e-1 5.0e-1 1
chr15 919 5.4e-1 2.6e-1 1
chr16 140 3.7e-1 8.4e-1 6.0e-2
chr17 27 2.3e-3 4.5e-3 2.4e-1
chr18 6 1 1 1
chr19 17 3.2e-2 8.0e-2 3.5e-2
chr20 3 1.3e-1 2.5e-1 3.0e-1
chr21 0 NA NA NA
chr22 166 0 (*) 1.3e-21 (*) 3.0e-1
chrX 2 1.4e-2 2.2e-1 1
chrY 1 2.9e-1 4.7e-1 1

# denotes the number of CNVs on that chromosome, 1.0e-2 stands for 1.0×102, and (*) denotes significance after Bonferroni adjustment at family-wise error rate (FWER) of 0.05.