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Norwegian population data for 15 autosomal STR loci

机译:15个常血糖str基因座的挪威人口数据

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Autosomal STR polymorphisms at 15 loci (D3S1358, THO1, D21S11, D18S51, Penta E, D5S818, D13S317, D7S820, D16S539, CSF1PO, Penta E, vWA, D8S1179, TPOX and FGA) are presented. Samples from current paternity analysis (( = 1380) were analysed. The observed heterozygosities ranged from 0.610 (TPOX) to 0 896 (Penta E). Two significant deviations from Hardy-Weinberg equilibrium were observed at D3S1352 and Penta D. The number of observed alleles ranged from 7 (THOl and TPOX) to 19 (D2IS 11 and FGA) The shortest tandem repeat observed was 2 2 at Penta D and the largest 44.2 at FGA The power of discrimination and exclusion ranged from 0.787 (TPOX) to 0.967 (FGA) and from 0.303 (TPOX) to 0.788 (Penta E) respectively. A complete frequency databases and other relevant forensic genetic parameters are presented.
机译:提出了15个基因座(D3S1358,THO1,D21S11,D18S51,PENTA E,D5S818,D13S317,D7S820,​​D16S539,CSF1PO,PENTA E,VWA,D8S1179,TPOX和FGA)。分析来自当前亲子率分析的样品((= 1380)。观察到的杂合子范围为0.610(TPOX)至0 896(Penta E)。在D3S1352和Penta D中观察到Hardy-Weinberg均衡的两种显着偏差。观察的数量从7(Thol和TPOX)到19(D2IS11和FGA)的等位基因在Penta D处的最短串联重复和在FGA的最大44.2的歧视和排除的力量范围为0.787(TPOX)至0.967(FGA )分别为0.303(TPOX)至0.788(PENTA E)。提出了完整的频率数据库和其他相关的法医基因参数。

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