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Table 2 Summary table of the suggestive linkage results

From: A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis

Maximum linkage scores of parametric linkage analysis
Chr 95 % C.I. (cM) Peak marker Locus HLOD (threshold) Alpha IC Diagnostic model Genetic model Empirical P value (threshold)
1 6.2 rs10919096 1q23.3 2.04 (1.97) 0.20 0.95 ASM3 Recessive 0.57 (0.632)
3 4.9 rs1001763 3p14.1 2.41 (1.97) 0.29 0.91 ASM3 Dominant 0.32 (0.632)
6 5.2 rs9381631 6p12.3 2.64 (1.97) 0.28 0.91 ASM3 Recessive 0.19 (0.632)
10 4.5 rs638395 10q26.2 2.25 (1.97) 0.28 0.93 ASM3 Recessive 0.40 (0.632)
  1. The table displays maximum linkage scores for the suggestive linkage results of the non-parametric and parametric linkage analyses
  2. A 1000-fold simulation analysis generated genome-wide thresholds for suggestive linkage Z and parametric HLOD scores (shown in parentheses). The approximate 95 % confidence intervals for the highest linkage scores are defined as a LOD-drop, or Z-drop, corresponding to a unit of 1.0. The mean information content (IC) estimate across all chromosomes was 0.92 (range 0.96–0.70), indicating that most of the genetic information was successfully captured using our high density mapping approach. The fraction of linked families, alpha, was less than 0.29 for regions showing suggestive linkage, indicating that there is evidence for a marked heterogeneity with respect to linked loci in these 46 pedigrees
  3. Abbreviations: NPL Z the linkage statistics for the estimation of identity-by-descent (IBD) allele sharing. LOD is the LOD calculated from NPL Z sores according to Kong and Cox (1997). IC the information content and is a measure of the probability that the IBD status at a certain locus can be determined for a given pairs of relatives. Alpha a measure of the locus heterogeneity that indicates the proportion of families with alleles linked to disease at a certain locus. HLOD estimate of the heterogeneity LOD score. Delta measure of allele sharing among affected individuals within pedigrees. Empirical P value estimated probability of having a score by chance that is at least as large as the observed one, after correction for multiple comparisons