Hi, Frank. Thanks for adding the extra tags; I hadn't seen your question. I also hesitate to post this as an answer because it really only posits some end-around options, but for what it's worth, here ya go:
Your being Big Y tested is extremely helpful and can be leveraged. One way is that testing single SNPs can provide actionable information. A big caveat here, however: it is not as comprehensive or definitive as chromosome full sequencing (of course), and you'll get no STR values from it. It will only give you one or a few, depending upon what's tested, points of comparison. But it is possible to correlate men who test positive to deep branches of the subclade.
It is also a highly targeted approach, not shotgunned. If there is solid reason to suspect a patrilineal relationship within the past several generations--I'd say five or six generations--it's doable. If there is no strong supposition and we just want someone to test because the surname is correct and there may be a connection, starting with a conventional 37-STR test would be a better approach. Inferring that this option can also be a bridge between a lower resolution test like the Y-37 and the comprehensive Big Y.
I should also mention here that this option really isn't very viable among some haplogroups. But in haplogroup R, which makes up over 47% of the 51,018 branches in FTDNA's current haplotree, there's a lot of granularity to work with so testing individual SNPs can convey a great deal of information.
FTDNA sells single and panel SNP tests, but only if you've already taken an STR test with them. Too, the catalog of individual SNPs doesn't always go very deep in some subclades. Test-takers can tell if selective SNP testing is available to them by looking at the haplogroup information from within their FTDNA dashboards. If they've only taken a Y-37 and are estimated to be M269, they'll see upgrades available for both panels of SNPs and individual SNPs.
YSEQ (https://yseq.net) in Germany, though, is more of an a la carte shop, and about half the FTDNA price for single SNPs (the cost is generally US$18 per SNP plus shipping). And they're very good quality. The owners, Thomas and Astrid Krahn sold their original company to FTDNA's parent, Gene by Gene, and were moved to Houston to help design and operationalize the lab here when processing shifted from the University of Arizona and brought in-house by FTDNA. After that was up and running well, the Krahns opted to move back to Germany and about a year afterward they opened YSEQ.
YSEQ doesn't strictly conform to FTDNA's haplotree nomenclature or branching, but they currently have 249,874 SNPs that can tested individually. And to think as recently as 2010 there were just over 800 SNPs total that had been identified on the Y chromosome. Mind boggling.
This means it requires some research to determine which SNPs you might want to order. Not from any best practices, just from personal experience with surname projects, my opinion is that there's a bit of a tightwire to walk. Testing too deeply right away may result in a negative result, making the test-taker feel like it's money thrown away and turning him off to additional testing attempts. Testing too high in the tree won't provide you strong evidence of any recent kinship: patrilineal line relatedness, yes; a connection in the last several generations, no.
My preferred approach is to balance cost with data detail. I'll generally choose two and sometimes three SNPs to recommend for testing together, choosing one of them high enough up your own subclades to have at least a 50/50 chance of a positive result. A single shipping charge plus three SNPs would be US$54, two SNPs US$36.
I did a little bit of the homework for you, but keep in mind that YSEQ may add SNPs to their catalog so this info is likely not to be comprehensive in a month or more. Too, I think this may end up displaying very poorly on G2G; but let's give it a shot. Using the data at FTDNA, you have a couple of subbranches under your own FT48099, so what I'll do is start at L48--11 branches above you--and it will be branch number 1. For each I'll use bold text to designate the FTDNA branch name, list all the associated or synonymous SNPs in each branch, and for the ones we know are cataloged and available for individual purchase, link to their respective pages at YSEQ:
- L48, FGC77285
- Y37962
- S23189, Y10968
- FT6679, FTA54130
- L200, FGC13729
- A11431, BY41679, FT7699, Y280633
- ACT920
- BY15306, BY15307, BY15309, BY15310, BY15311, BY15312, BY15313, BY15317, BY41918, FT10008, FT265844, FT7070, FT7456, FT8081
- BY15314, BY15316
- BY92194, BY104823, BY127393, BY130692, BY133868, BY138588, BY150626, BY156900, BY222867, FT45577, FT47732, FT47739, FT9613
- FT8553, FT9818
- FT48099, FT178539, FT47090, FT47202, FT47309, FT47418, FT48362
- FT8982
- FT267444, FT267609, FT267617
- FT308562, FT308851, FT309960, FT310099, FT351866, FT354128, M4179
Last up, all of our common autosomal DNA tests--with the exception of those from FTDNA because, well, a for-purpose yDNA makes more sense there--include Y-SNPs in their arrays. Living DNA and 23andMe report those results, but the others, like AncestryDNA and MyHeritage do not.
That's kind of a crap shoot because we don't which of your relevant SNPs may be tested below M269, and each company and even version of each test can differ (my bet is that most will test to at least U106). If you have autosomal DNA matches you're confident are on your patrilineal line, and they don't have yDNA information from the testing company, getting them to check the Y-SNPs in the raw data can be a useful way to at least weed out those you know won't benefit from yDNA testing or single SNP testing. "Benefit" in that sense, of course, meaning your goal for Blankenship tracing. If you aren't familiar with how you can obtain yDNA information from AncestryDNA and MyHeritage tests, let me know.