Paternal Haplotype
CRI
Note: From what I understand there are two methods of naming haplogroups. One is by types of mutations called single-nucleotide polymorphisms (SNP's) which would have meaning to those who study DNA but not to amateurs such as myself. The other is by phylogenetic tree ("family tree") which is more understandable to people like me. Thus haplogroup M207 (R) has mutations M173 ((R1) and M479 (R2). Further mutations of R1, are for example M420 (R1a) and M342 (R1b), and so on. Since different companies give results using one or the other method, comparison of results can certainly be confusing to many consumers.
CRI gives my haplogroup as R1b and 23andMe gives it as R-M269 with further mutations to the subclade R-CTS9881. In fact they agree, however the 23andMe result is much more specific. R-M269 is also known as R1b1a1b. I haven't been able to determine the phylogenetic name for R-CTS9881, if there is one.
Haplogroup R-M269 (R1b1a1b) is the most frequently occurring paternal lineage in Europe carried by an estimated 110 million males in Europe and, of course, by many of us of European descent. 23andMe suggests my subclade is quite rare and is often found (but not exclusively) in males whose with roots are in northwestern Ireland and is common with those in the Ui Neill dynasty. 23andMe indicates this subclade is found in only 1 in 5100 male customers. Amongst the 5000 closest DNA relatives indicated by 23andMe none of those males share my paternal Haplogroup, which may be disappointing, but based on the math, not surprising.