Brown - FTDNA - 

FTDNA autosomal match "????cm" to Ballard with family finder SNP designation R-S1211 (Adrian Ballard's male Y line) [Source].

37 STR test - 4 step

MtDNA Haplogroup: 

FTDNA reported Relationship Range estimates "

of Norfolk ?

recorded at FTDNA 

Y DNA test required

May be a different tester but my belief with the information currently avaliable these results belong to sample; "Brown" or "Mamgren"

37 STR

IN147845 - Unknown ? Unknown Origin R-S1211 Family Finder

Sample comparison; at 37 STR

IN147845

13 24 14 11 11-14 12 12 11 13 13 29 16  9-10 11 11 25 15 19 31 16-16-16-17 10 11 19-23 16 15 18 14 36-37 12 12

258423 - Ballard

13 24 14 10 11-14 12 12 11 13 13 29  17 9-10 11 11 25 15 19 30 16-16-16-17 10 11 19-23 16 15 18 15 36-37 12 12

IN91033 - Ballard

13 24 14 10 11-14 12 12 11 13 13 29  17 9-10 11 11 25 15 19 30 16-16-16-17 10 11 19-23 16 15 18 16 36-37 12 12

Family Finder SNP

CTS10149+, CTS10362+, CTS10834+, CTS109+, CTS11358+, CTS125+, CTS12632+, CTS196+, CTS1996+, CTS2466+, CTS2664+, CTS3063+, CTS3135+, CTS3229+, CTS3316+, CTS3358+, CTS3431+, CTS3446+, CTS3475+, CTS3536+, CTS3575+, CTS3622+, CTS3654+, CTS3662+, CTS3868+, CTS4244+, CTS4364+, CTS4368+, CTS4437+, CTS4528+, CTS4740+, CTS5318+, CTS5418+, CTS5532+, CTS5808+, CTS5884+, CTS623+, CTS6383+, CTS6800+, CTS6832+, CTS7194+, CTS7604+, CTS7904+, CTS8243+, CTS8436+, CTS8612+, CTS8626+, CTS8627+, CTS8980+, CTS9014+, CTS9722+, CTS9828+, F115+, F1209+, F1329+, F1704+, F1714+, F1753+, F1767+, F2048+, F2142+, F2155+, F2402+, F2587+, F2837+, F3111+, F313+, F3136+, F3556+, F47+, F719+, F82+, FGC58+, FT3312+, L1002+, L1004+, L1009+, L1013+, L1053+, L11+, L1112+, L1116+, L1185+, L132+, L1348+, L1351+, L1480+, L15+, L151+, L16+, L23+, L265+, L278+, L350+, L352+, L389+, L407+, L470+, L479+, L482+, L483+, L498+, L500+, L502+, L508+, L51+, L52+, L585+, L741+, L747+, L752+, L753+, L754+, L757+, L761+, L768+, L773+, L779+, L82+, L989+, M11301+, M168+, M173+, M207+, M213+, M269+, M294+, M306+, M343+, M415+, M42+, M45+, M526+, M5590+, M5597+, M5607+, M5609+, M5610+, M5613+, M5615+, M5624+, M5625+, M5627+, M5629+, M5632+, M5633+, M5636+, M5649+, M5650+, M5652+, M5657+, M5662+, M5681+, M5682+, M5692+, M5697+, M5708+, M5709+, M5712+, M5726+, M5738+, M5747+, M5775+, M5777+, M5783+, M5788+, M5791+, M5812+, M5821+, M5825+, M89+, M9+, M94+, P128+, P131+, P132+, P135+, P136+, P138+, P139+, P14+, P140+, P141+, P143+, P145+, P146+, P148+, P149+, P151+, P157+, P158+, P159+, P160+, P163+, P166+, P224+, P225+, P226+, P228+, P229+, P230+, P232+, P233+, P234+, P235+, P236+, P237+, P238+, P239+, P240+, P242+, P243+, P244+, P245+, P25+, P280+, P281+, P282+, P283+, P284+, P285+, P295+, P297+, P305+, P310+, P311+, PAGES00026+, PAGES00083+, PF1016+, PF1029+, PF1040+, PF1046+, PF1061+, PF1092+, PF1097+, PF1203+, PF1415+, PF210+, PF223+, PF234+, PF258+, PF2591+, PF2600+, PF2608+, PF2614+, PF2615+, PF2620+, PF2624+, PF263+, PF2718+, PF272+, PF2723+, PF2739+, PF2745+, PF2747+, PF2748+, PF278+, PF292+, PF325+, PF342+, PF3495+, PF5459+, PF5490+, PF5495+, PF5500+, PF5503+, PF5862+, PF5865+, PF5869+, PF5872+, PF5881+, PF5885+, PF5886+, PF5889+, PF5936+, PF5945+, PF5953+, PF5957+, PF5964+, PF5978+, PF5980+, PF5981+, PF5982+, PF5984+, PF6091+, PF6145+, PF6249+, PF6250+, PF6265+, PF6271+, PF6272+, PF6399+, PF6409+, PF6426+, PF6429+, PF6430+, PF6432+, PF6434+, PF6435+, PF6437+, PF6443+, PF6452+, PF6463+, PF6469+, PF6470+, PF6477+, PF6479+, PF6494+, PF6495+, PF6498+, PF6500+, PF6506+, PF6507+, PF6509+, PF6520+, PF6524+, PF719+, PF779+, PF815+, PF840+, PF844+, PF892+, PF937+, PF951+, PF970+, S1196+, S1211+, S14328+, s3+, V168+, V171+, V174+, V189+, V205+, V221+, V241+, V250+, V2590+, V52+, V9+, Y1493+, Y1526+, Y1571+, Y441+, Y8291+, YSC0000075+, YSC0000186+, YSC0000191+, YSC0000224+, YSC0000225+, YSC0000227+, YSC0000269+, YSC0000288+, Z11893+, Z11917+, Z17709+, A702+, AF4-, S15363-, S24014-

N147845

Unknown Origin

H1-T16189C!

H1a99a1

A16129G, A16183c, T16187C, T16223C, G16230A, T16278C, C16311T

C146T, C152T, A153G, A247G, 522.1A, 522.2C, 315.1C

Dirk Struve STR dating calculation - A simple back on the envelope calculation: On the 111 marker scale 1 marker counts as 162 years assuming 32 years of generation time. So 17 steps equals roughly 2.800 years. This must be divided by 2 because both samples moved away from the same ancient ancestor. Thus the ancestor lived about 1.400 years ago = 600 CE. Because mutations happen by chance we must apply some statistics to get a confidence interval. For a Gaussian distribution this is the square_root of the number of mutations for 68% confidence and double of this for 95% confidence which is most often used in population genetics. In the end we get the result that the ancestor lived about 600 CE plus/minus 650 years with 95% confidence (-50 BCE - 1.250 CE). Needless to say that this is a huge uncertainty and indeed is does not make much sense to compare only 2 persons on a 111 marker scale. Good online calculators use Poisson statistics instead of Gaussian statistics which is a bit more precise and take into account that STR markers saturate (move back and forth so that many mutations are no longer visible) but that does not fix the general problem with STR markers. That is also the reason why FTDNA limits the number of mutations for their calculation.