If you think this was unprovoked look again. This is your post #158:
That sentence was totally unnecessary, and I told you I have 0 tolerance for condescension. If you or anyone else doesn't see a problem with that then you are totally tone deaf. You could have posted that without sounding like an asshole, and it would have been fine. We wouldn't be at this point now. I told you in the previous post I have delt with slights in the past but not anymore! You say you are not asking for a fight. Those are fighting words to me. You have no business making authoritative statements like "nonsense". The only time I use that word is when I'm discussing Afrocentrism or historical revisionism. There's far more wiggle room with DNA tools.
And on your statement with AHG. It does have levantine affintity. This is from Feldman et al. 2019
https://www.nature.com/articles/s41467-019-09209-7
Inspired by our qualitative observations in PCA and ADMIXTURE analyses, we applied formal statistical frameworks to describe the genetic profiles of the three Anatolian populations and to test and model genetic differences between them. We first characterized the ancestry of AHG. As expected from AHG’s intermediate position on PCA between Epipaleolithic/Neolithic Levantines and WHG, Patterson’s D-statistics13 of the form D (AHG, WHG; Natufian/Levant_N, Mbuti) ≥ 4.8 SE (standard error) and D (AHG, Natufian/Levant_N; WHG, Mbuti) ≥ 9.0 SE (Supplementary Table 3) indicate that AHG is distinct from both the WHG and Epipaleolithic/Neolithic Levantine populations and yet shares extra affinity with each when compared to the other. Then, we applied a qpAdm-based admixture modeling to integrate these D- statistics. qpAdm is a generalization of D/f4-statistics that test whether the target population and the admixture model (i.e., a linear combination of reference populations) are symmetrically related to multiple outgroups13. By doing so, it tests whether the proposed admixture model is adequate to explain the target gene pool and provides admixture coefficient estimates. We find an adequate two-way admixture model (χ2p = 0.158), in which AHG derives around half of his ancestry from a Neolithic Levantine-related gene pool (48.0 ± 4.5%; estimate ± 1 SE) and the rest from the WHG-related one (Supplementary Tables 4, 5). While these results do not suggest that the AHG gene pool originated as a mixture of Levant_N and WHG, both of which lived millennia later than AHG, it still robustly supports that AHG is genetically intermediate between WHG and Levant_N. This cannot be explained without gene flow between the ancestral gene pools of those three groups. This supports a late Pleistocene presence of both Near-Eastern and European hunter-gatherer-related ancestries in central Anatolia. Notably, this genetic link with the Levant pre-dates the advent of farming in this region by at least five millennia.