The rationale for the different benefits from Technique I and Method II in the case of siblings and double cousins would be that the cM lengths exhibited by FTDNA and in the cost-free GEDmatch utility (and, certainly, 23andMe's own Family Inheritance: Sophisticated) do not distinguish involving fifty percent-equivalent and completely identical areas.
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23andMe consist of the X-chromosome in their calculations, so their cM figures is going to be larger than All those supplied by FTDNA. 23andMe built adjustments towards the cM rely in June 2013 so the amount of cMs will fluctuate a little bit based on if the exam was taken.
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You should see the first sources for more in depth information and facts. These statistics are up to date yearly and as new info is released.)
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Due to the random way that autosomal DNA is inherited, third, fourth plus more distant cousins will not essentially have any detectable half-equivalent regions. In line with Relatives Tree DNA's figures You will find a ninety% probability that 3rd cousins will share ample DNA for the relationship for being detected, but there's just a fifty% probability that you'll share plenty of DNA with a fourth cousin for the connection to be determined.